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(a) Nakata, T.; Nomura, S.; Matsukura, H. Tetrahedron Lett. 1996, 37, 213.
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(d) Nagasawa, K.; Hori, N.; Shiba, R.; Nakata, T. Heterocycles 1997, 44, 105.
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(e) Nagasawa, K.; Hori, N.; Koshino, H.; Nakata, T. Heterocycles 1999, 50, 919.
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(a) Hori, N.; Nagasawa, K.; Shimizu, T.; Nakata, T. Tetrahedron Lett. 1999, 40, 2145.
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(b) Shimizu, T.; Hiranuma, S.; Nakata, T. Tetrahedron Lett. 1996, 37, 6145.
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(c) Shimizu, T.; Ohzeki, T.; Hiramoto, K.; Hori, N.; Nakata, T. Synthesis 1999, 1373.
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Morimoto, M.; Matsukura, H.; Nakata, T. Tetrahedron Lett. 1996, 37, 6365.
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17
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0030489899
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1,4-and 1,5-Rearrangement-ring expansion of oxiranes via bicyclo-[3.1.0] and [4.1.0]oxonium ions, respectively, were reported, (a) Hayashi, N.; Fujiwara, K.; Murai, A. Chem. Lett. 1996, 341.
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(b) Hayashi, N.; Fujiwara, K.; Murai, A. Tetrahedron Lett. 1996, 37, 6173.
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(e) Fujiwara, K.; Hayashi, N.; Tokiwano, T.; Murai, A. Heterocycles 1999, 50, 561.
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(f) Hayashi, N.; Noguchi, H.; Tsuboi, S. Tetrahedron 2000, 56, 7123.
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Hayashi, N.1
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(a) Kamada, T.; Ge-Qing; Abe, M.; Oku, A. J. Chem. Soc., Perkin Trans. 1 1996, 413.
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(b) Mukai, C.; Yamashita, H.; Ichiryu, T.; Hanaoka, M. Tetrahedron 2000, 56, 2203.
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0043045262
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28
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0000887154
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(c) Blumenkopf, T. A.; Bratz, M.; Castañeda, A.; Look, G. C.; Overman, L. E.; Rodriguez, D.; Thompson, A. S. J. Am. Chem. Soc. 1990, 112, 4386.
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Overman, L.E.5
Rodriguez, D.6
Thompson, A.S.7
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29
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85034523626
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2 at 0°C. See ref 12 for preparation of 10b
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2 at 0°C. See ref 12 for preparation of 10b.
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30
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0009949622
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Alcohol 10b was prepared by a known procedure; see: Hornberger, C. S., Jr.; Heitmiller, R. F.; Gunsalus, I. C.; Schnakenberg, G. H. F.; Reed, L. J. J. Am. Chem. Soc. 1953, 75, 1273.
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Hornberger C.S. Jr.1
2
Heitmiller, R.F.3
Gunsalus, I.C.4
Schnakenberg, G.H.F.5
Reed, L.J.6
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31
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85034523721
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note
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3) δ 74.3, 71.7, 33.9, 32.7, 22.0.
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32
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85034525782
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1H NMR spectrum analysis of the diastereomeric mixture of their (R)-MTPA ester derivatives. This result indicates that 23b was produced via meso-bicyclooxonium ion intermediate 22
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1H NMR spectrum analysis of the diastereomeric mixture of their (R)-MTPA ester derivatives. This result indicates that 23b was produced via meso-bicyclooxonium ion intermediate 22.
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